Human Apolipoprotein E ε4 Allele Modulates Energy Substrate Availability, Seizure Burden, Mortality and Hippocampal Injury, Cell Death, and Inflammation after Neonatal Hypoxic-Ischemic Brain Injury

Humanized ApoE4, compared to ApoE3, causes greater hippocampal injury, cell death, and inflammation after a neonatal HI insult in association with low BG and underutilized KB. The mechanisms behind these associations need further investigation.

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Publication Details

Journal
Developmental Neuroscience
Published
2025-09-16
DOI
https://doi.org/10.1159/000548432
Primary Topic
Neonatal and fetal brain pathology
Type
article
Field-Weighted Citation Impact
0.00
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article

Human Apolipoprotein E ε4 Allele Modulates Energy Substrate Availability, Seizure Burden, Mortality and Hippocampal Injury, Cell Death, and Inflammation after Neonatal Hypoxic-Ischemic Brain Injury

M Pierre, Frances J. Northington, Michelle Nazareth, Lee J. Martin et al.
Developmental Neuroscience
Neonatal and fetal brain pathology
article

Human Apolipoprotein E ε4 Allele Modulates Energy Substrate Availability, Seizure Burden, Mortality and Hippocampal Injury, Cell Death, and Inflammation after Neonatal Hypoxic-Ischemic Brain Injury

M Pierre, Frances J. Northington, Michelle Nazareth, Lee J. Martin, Lauren L. Jantzie, Charles Lechner, Sarah Ann Duck, Susan J. Vannucci, Raul Chavez‐Valdez, Charles Pinto, Abigail Fassinger, Genesis Elmore, Michael Nugent
article en

Abstract

Humanized ApoE4, compared to ApoE3, causes greater hippocampal injury, cell death, and inflammation after a neonatal HI insult in association with low BG and underutilized KB. The mechanisms behind these associations need further investigation.

Developmental Neuroscience
Kennedy Krieger Institute (US), Johns Hopkins University (US), University of Toronto (CA), Cornell University (US), Johns Hopkins Medicine (US), MIND Research Institute (US)
Openalex Percentile: Top 65%
Neonatal and fetal brain pathology
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